K-number	K082506
Device name	SYMBIA, VERSION 4.0
Applicant	Siemens Medical Solutions USA, Inc.
Product code	KPS
Device class	Class II
Decision date	Nov 21, 2008
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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SYMBIA, VERSION 4.0

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